Production Supervisor, Packaging

The Supervisor, Production is responsible for all aspects of a specific shift within the Transdermal Manufacturing and Packaging facility, including ensuring that all work is performed in compliance with Safe Work Practices, cGMP, Standard Operating Procedures, and company policies.  As part of the Production leadership team, the main focus is responsibility for day-to-day performance and results, developing systems and measurements to evaluate area performance and employee individual performance and contribution and lead initiatives (e.g. reliability) to facilitate improved productivity.

• Works as a member of a team to achieve all outcomes.

• Provide results oriented leadership that drives continuous improvement consistent with the Operations Strategic Plan and the Production Plan, including commercial and R&D MFG and PKG operations.

• Co-ordinate, assign and supervise all production activities and outcomes for area of responsibility to ensure production schedule/agreed upon goals and objectives are met.

• Develop systems and metrics to measure and evaluate both productivity and individual performance and contribution on an on-going basis.

• Use systems and metrics to guide the initiation and execution of safety, quality, productivity and continuous improvement initiatives in support of the Operations Strategic Plan and Production Plan.

• Provide strong leadership to the team that fosters personal development,   interaction and participation.

• Provide leadership as a member of the Production leadership team, building  and maintaining positive relationships with the key business partners within       and outside of Production (e.g. Engineering, Technical Services,  Warehouse,      Materials, Warehouse, QA, Formulations, Human Resources etc.)

• Ensure department is professional and performs all work in accordance with all       established regulatory, compliance and safety requirements. Initiate investigations and provide or implement preventive/corrective action for all safety and compliance non-conformances.

• Ensures that all production areas and equipment are kept neat, clean and organized at all times.

• Responsible for the security of the building and company assets after normal business hours and in addition, directly responsible for all Aveva DDS employees after normal business hours.

• Provide recommendations to the next level of management regarding procedural and organizational changes.  Writes and.or revises batch records, SOPs, Work Instructions and investigates and writes investigation reports as needed.

• Evaluate the individual performance and contribution of all direct reports on       an on-going basis and establish developmental plans in conjunction with individuals where required.  Ensure employees participate/receive all relevant       training within required timeframes.

• Interviews prospective candidates, evaluates temporary personnel and provides input for the hiring process of permanent employees.

• Responsible for selecting designated observers for controlled substance materials.

• Responsible for the resolution of all employee issues within the department with the involvement of the next level of management and human resources as  required.

• Acts as a specialized manufacturing resource to senior management to support resolution of complex issues.

• Recruits, trains, develops and manages effectively the ongoing performance of their direct reports, which includes, but is not limited to:
  • Reviewing and updating development plans for all direct reports, ensuring that all direct reports are properly trained and qualified according to our  Training and Employee Qualification Enterprise Policy;
  • Effectively managing performance for direct reports according to the  Performance Management Program,
  • Attracting and retaining talent based on our talent management framework;
  • Scheduling regular one-on